Summary
Overview
Work History
Education
Skills
Clinical trial Experience
Languages
Timeline
Generic

YEEUN Park

Gwanak-gu, Seoul

Summary

Proven Clinical Research Assistant with a track record of enhancing patient recruitment and retention by over 30% at Korea Cancer Study Group. Expert in Clinical Data Management and adept at fostering study team relationships, ensuring meticulous adherence to protocol development and regulatory guidelines. Ethical Clinical Research Assistant bringing 2 years of research industry performance to add value to Your team. Adept at monitoring pharmaceutical sponsor compliance and ethical guidelines to foster seamless clinical trial operations. Highly organized and thorough with good planning and problem-solving abilities. Knowledgeable Clinical Research Associate adept at recognizing clinical values and abstract data from source documents. Uses analytical skills to identify data or patient safety issues. Reliable Medical Support professional with 2 years of experience in Clinical Study environment. Organized CRA with foundation in records management. Detail-oriented team player with strong organizational skills. Ability to handle multiple projects simultaneously with a high degree of accuracy. To seek and maintain full-time position that offers professional challenges utilizing interpersonal skills, excellent time management and problem-solving skills. Organized and dependable candidate successful at managing multiple priorities with a positive attitude. Willingness to take on added responsibilities to meet team goals.

Overview

2
2
years of professional experience

Work History

Clinical Research Assistant

Korea Cancer Study Group
2023.06 - Current
  • Participated in site monitoring visits, addressing any concerns or discrepancies related to patient enrollment or data collection procedures.
  • Maintained up-to-date knowledge of industry regulations by attending professional development seminars and reviewing relevant publications regularly.
  • Monitored safety events during clinical trials by promptly reporting adverse events and implementing corrective action plans as needed.
  • Facilitated efficient organization of study-related documents through meticulous record-keeping practices.
  • Educated patients regarding all facets of clinical study participation.
  • Developed strong relationships with patients through compassionate care coordination during their participation in clinical studies.
  • Improved patient retention rates in longitudinal studies by establishing rapport with participants and maintaining regular follow-up communication throughout trial duration.
  • Enhanced patient recruitment by developing targeted outreach strategies and materials for clinical trials.
  • Conducted literature reviews to inform study designs and enhance understanding of current trends in clinical research.
  • Assisted with research protocol development.
  • Supported investigators with the design and implementation of study protocols, ensuring adherence to regulations and ethical guidelines.
  • Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.

Clinical-research-assistant

The Way Healthcare
2022.03 - 2023.05
  • Participated in site monitoring visits, addressing any concerns or discrepancies related to patient enrollment or data collection procedures.
  • Monitored safety events during clinical trials by promptly reporting adverse events and implementing corrective action plans as needed.
  • Facilitated efficient organization of study-related documents through meticulous record-keeping practices.
  • Educated patients regarding all facets of clinical study participation.
  • Developed strong relationships with patients through compassionate care coordination during their participation in clinical studies.
  • Improved patient retention rates in longitudinal studies by establishing rapport with participants and maintaining regular follow-up communication throughout trial duration.
  • Enhanced patient recruitment by developing targeted outreach strategies and materials for clinical trials.
  • Provided training to new team members on proper procedures for data collection, documentation, and reporting in clinical trials.
  • Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
  • Assisted with research protocol development.
  • Supported investigators with the design and implementation of study protocols, ensuring adherence to regulations and ethical guidelines.
  • Expedited study progress by overseeing timely completion and submission of required documents, forms, and reports in accordance with regulatory guidelines.

Education

Bachelor of Science - Biology

Kangwon National University
Chuncheon, South Korea
02.2014

Skills

  • Electronic Data Capture
  • Informed Consent Process
  • Adverse event reporting
  • Clinical trial management
  • Clinical Data Management
  • Site Management
  • Source Document Verification
  • Subject Retention Strategies
  • Protocol development
  • IRB Submissions
  • Documentation Management
  • Research SOPs understanding
  • Quality Control

Clinical trial Experience

-Breast Cancer/IIT/2023.06~Ongoing

-Advanced Solid Tumor/IIT/2023.06~Ongoing

-NSCLC/IIT/2023.06~Ongoing

-Salivary Gland Cancer/IIT/2023.06~Ongoing

-Mild Cognitive Impairment(Digital Therapeutics)/ SIT/ Phase II/ 2022.11~2023.05

-Visual Field Defect Caused by Brain Disease(Digital Therapeutics)/ SIT/ Phase II/ 2022.11~2023.05

-Echocardiography/IIT/National Project/2022.06~2023.05

-Hyperlipidemia/SIT/Observation Study/2022.06~2023.05

-Dyslipidemia/SIT/Observation Study/

-Polyuria/SIT/Phase IV/2022.04~2023.05

-Chronic Prostatitis/SIT/Phase IV/2022.04~2023.05

Languages

Korean
Native language
English
Elementary
A2

Timeline

Clinical Research Assistant

Korea Cancer Study Group
2023.06 - Current

Clinical-research-assistant

The Way Healthcare
2022.03 - 2023.05

Bachelor of Science - Biology

Kangwon National University
YEEUN Park